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1.
Vaccine ; 42(24): 126209, 2024 Oct 24.
Artigo em Inglês | MEDLINE | ID: mdl-39217777

RESUMO

BACKGROUND: Pneumococcus is a common cause of pneumonia, meningitis, and other serious infections in children. The previous study has proved that the 13-valent pneumococcal conjugate vaccine (PCV13) has sufficient immunogenicity in children. The data on long-term persistence of immunity will help the follow-up development work of pneumococcal vaccines. METHODS: Children who received the full vaccination course of the tested PCV13 in the previous clinical trial were enrolled again, and these who received other pneumococcal vaccines, or were infected with one or more serotypes of S. pneumoniae corresponding to PCV13 before enrollment were excluded. Participants were divided into four groups by age which is same as that of previous trial. The study lasted for 5 years, during which we measured pneumococcal antibodies of 13 serotypes included in PCV13 at particular points in time. Geometric mean concentrations (GMCs) and seropositive rates (the rate of IgG concentration ≥0.35 µg/mL) of antibodies against 13 serotypes were calculated. RESULTS: For the participants aged 2 months, five years after primary vaccination, except for serotypes 3 and 4, seropositive rates were 100%. GMCs of IgG antibodies against 13 serotypes ranged from 0.733 to 15.160 µg/mL. All of the participants aged 7-11 months had the serotype-specific IgG concentration ≥0.35 µg/mL four years after primary vaccination with the exception of serotypes 3, 4, 6 A and 9 V. IgG GMCs were 0.753-11.031 µg/mL. All participants aged 12-23 months and 2-5 years old had the serotype-specific IgG concentration ≥0.35 µg/mL three or two years after primary vaccination respectively, except for serotype 3. IgG GMCs ranged from 0.815 to 13.111 µg/mL, and 0.684 to 12.282 µg/mL respectively. CONCLUSION: PCV13 was applied to the population aged 2 months and 7 months - 5 years old with a good immune persistence, providing more extensive evidence of long-term efficacy for that vaccine. TRIAL REGISTRATION: The trial was registered with ClinicalTrials.gov, number NCT06210737.


Assuntos
Anticorpos Antibacterianos , Imunoglobulina G , Infecções Pneumocócicas , Vacinas Pneumocócicas , Sorogrupo , Streptococcus pneumoniae , Humanos , Vacinas Pneumocócicas/imunologia , Vacinas Pneumocócicas/administração & dosagem , Lactente , Anticorpos Antibacterianos/sangue , Anticorpos Antibacterianos/imunologia , Pré-Escolar , Streptococcus pneumoniae/imunologia , Streptococcus pneumoniae/classificação , Feminino , Masculino , Infecções Pneumocócicas/prevenção & controle , Infecções Pneumocócicas/imunologia , Imunoglobulina G/sangue , Imunoglobulina G/imunologia , Vacinas Conjugadas/imunologia , Vacinas Conjugadas/administração & dosagem , Vacinação/métodos
2.
Chem Biodivers ; 19(3): e202100990, 2022 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-35083850

RESUMO

Two new decalin derivatives named fusarielins O (1) and P (2), together with seven known compounds (3-9) were isolated from the crude extract of the marine-derived fungus Talaromyces sp. The planar structures of the new compounds were elucidated by comprehensive spectroscopic analyses of NMR and HR-ESI-MS. The absolute configuration of 1 was assigned by Snatzke's method and comparison of experimental and calculated electronic circular dichroism (ECD) spectra. Compounds 1-9 were evaluated for their cytotoxic activities against three tumor cell lines and 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical scavenging activities.


Assuntos
Antineoplásicos , Talaromyces , Antineoplásicos/química , Dicroísmo Circular , Estrutura Molecular , Naftalenos , Talaromyces/química
3.
Mar Drugs ; 19(4)2021 Mar 27.
Artigo em Inglês | MEDLINE | ID: mdl-33801640

RESUMO

Three new andrastin-type meroterpenoids penimeroterpenoids A-C (1-3) together with two known analogs (4 and 5) were isolated from the cultures of the marine-derived Penicillium species (sp.). The structures of the new compounds were elucidated on the basis of 1- and 2-dimensional (1D/2D) Nuclear Magnetic Resonance (NMR) spectroscopic and mass spectrometric analysis. The absolute configurations of 1-3 were determined by comparison of experimental and calculated electronic circular dichroism (ECD) spectra. Compound 1 showed moderate cytotoxicity against A549, HCT116, and SW480 cell lines.


Assuntos
Androstadienos/farmacologia , Antineoplásicos/farmacologia , Neoplasias/tratamento farmacológico , Penicillium/metabolismo , Terpenos/farmacologia , Células A549 , Androstadienos/isolamento & purificação , Antineoplásicos/isolamento & purificação , Sobrevivência Celular/efeitos dos fármacos , Células HCT116 , Células HeLa , Humanos , Células MCF-7 , Estrutura Molecular , Neoplasias/patologia , Relação Estrutura-Atividade , Terpenos/isolamento & purificação
4.
Front Microbiol ; 12: 641504, 2021.
Artigo em Inglês | MEDLINE | ID: mdl-33868199

RESUMO

Three new secondary metabolites pestalothenins A-C (1-3), including two new humulane-derived sesquiterpeniods (1 and 2) and one new caryophyllene-derived sesquiterpeniod (3), together with five known compounds (4-8) were isolated from the crude extract of the plant endophytic fungus Pestalotiopsis theae (N635). Their structures were elucidated by the extensive analyses of HRESIMS and NMR spectroscopic data. The absolute configurations of 1-3 were determined by comparison of experimental and calculated electronic circular dichroism (ECD) spectra. The cytotoxic effects of these compounds were evaluated in vitro. Compound 6 showed moderate cytotoxicity against T24 and MCF7 cell lines. In addition, compounds 1-8 were also evaluated for antibacterial activity.

5.
J Antibiot (Tokyo) ; 74(2): 152-155, 2021 02.
Artigo em Inglês | MEDLINE | ID: mdl-32843724

RESUMO

One new chromanone derivative, alterchromanone A (1), and four known curvularin-type macrolides (2-5) were isolated from the crude extract of the mangrove-derived endophytic fungus Alternaria longipes. Their structures were elucidated by MS and NMR spectroscopic analyses and by a comparison with data from the literature. The absolute configuration of 1 was assigned by combination of experimental and calculated electronic circular dichroism (ECD) spectra. Compound 1 exhibited 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical scavenging activity with an IC50 value of 56.3 µg ml-1. According to the structural features of these compounds, the plausible biosynthetic pathways of 1-5 were also proposed.


Assuntos
Alternaria/química , Sequestradores de Radicais Livres/farmacologia , Rhizophoraceae/microbiologia , Antioxidantes/farmacologia , Compostos de Bifenilo/química , Dicroísmo Circular , Endófitos/química , Espectroscopia de Ressonância Magnética , Espectrometria de Massas , Estrutura Molecular , Picratos/química
6.
Sci Rep ; 10(1): 15812, 2020 09 25.
Artigo em Inglês | MEDLINE | ID: mdl-32978439

RESUMO

Potassium (K) is essential for plant growth and stress responses. MicroRNAs (miRNAs) are involved in adaptation to nutrient deprivation through modulating gene expression. Here, we identified the miRNAs responsive to K deficiency in Triticum aestivum based on high-throughput small RNA sequencing analyses. Eighty-nine miRNAs, including 68 previously reported ones and 21 novel ones, displayed differential expression under K deficiency. In Gene Ontology and Kyoto Encyclopedia and Genome analyses, the putative target genes of the differentially expressed miRNAs were categorized into functional groups associated with ADP-binding activity, secondary metabolic pathways, and biosynthesis and metabolism. Functional characterization of tae-miR408, an miRNA significantly down-regulated under K deficiency, revealed its important role in mediating low-K tolerance. Compared with wild type, transgenic tobacco lines overexpressing tae-miR408 showed significantly improved K uptake, biomass, photosynthesis, and reactive oxygen species scavenging under K deficiency. These results show that distinct miRNAs function in the plant response to K deficiency through regulating target genes involved in energy metabolism and various secondary metabolic pathways. Our findings shed light on the plant response to K deficiency mediated by miRNAs in T. aestivum. Distinct miRNAs, such as tae-miR408, are valuable targets for generating crop varieties with improved K-use efficiency.


Assuntos
Regulação da Expressão Gênica de Plantas , MicroRNAs/genética , Proteínas de Plantas/metabolismo , Potássio/metabolismo , RNA de Plantas/análise , Triticum/metabolismo , Perfilação da Expressão Gênica , Sequenciamento de Nucleotídeos em Larga Escala , MicroRNAs/metabolismo , Proteínas de Plantas/genética , Plantas Geneticamente Modificadas/genética , Plantas Geneticamente Modificadas/metabolismo , RNA de Plantas/genética , Nicotiana/genética , Nicotiana/metabolismo , Triticum/genética , Triticum/crescimento & desenvolvimento
7.
Chin J Nat Med ; 18(4): 261-267, 2020 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-32402402

RESUMO

Two new caryophyllene-type sesquiterpenoids, pestathenols A (1) and B (2) and one new α-furanone, pestatheranone A (6), along with five known compounds (3-5, 7 and 8) have been isolated from the crude extract of the plant endophytic fungus Pestalotiopsis theae. Their structures were unambiguously established by extensive spectroscopic analyses. The absolute configuration of the 5,6-diol moiety in 1 was assigned using Snatzke's method. Compounds 1 and 2 showed weak cytotoxicity against HeLa cell line.


Assuntos
Furanos/química , Pestalotiopsis/química , Extratos Vegetais/química , Sesquiterpenos Policíclicos/química , Sesquiterpenos/química , Furanos/isolamento & purificação , Células HeLa , Humanos , Estrutura Molecular , Sesquiterpenos Policíclicos/isolamento & purificação , Sesquiterpenos/isolamento & purificação
8.
RSC Adv ; 10(66): 40384-40390, 2020 Nov 02.
Artigo em Inglês | MEDLINE | ID: mdl-35520825

RESUMO

Pycnidiophorones A-D (1-4), four new cytochalasans with a rare 5/6/6/5/6 pentacyclic skeleton incorporating the unique 12-oxatricyclo[6.3.1.02,7]dodecane core, and six known depsidones (5-10) were isolated from cultures of the wetland-soil-derived fungus Pycnidiophora dispersa. Their chemical structures were unambiguously determined using NMR spectroscopic data. The absolute configurations of 1 and 3 were assigned by electronic circular dichroism (ECD) calculations. Compounds 1-10 showed moderate cytotoxicity against a panel of five human tumor cell lines.

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